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Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse mmodel and humans with Prader-Willi Syndrome.

Research group Swaab
Publication year 2013
Published in PLoS Genetics
Authors A. Rieusset, F. Schaller, U.A. Unmehopa, V. Matarazzo, F. Watrin, M. Linke, B. Georges, J. Bischof, Feike A. Dijkstra, M. Bloemsma, S. Corby, F.J. Michel, R. Wevrick, U. Zechner, D.F. Swaab, K. Dudley, L. Bezin, F. Muscatelli

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